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Jennifer Just

Showing results (11-20 of 15) with videos related to

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Orphanet Journal of Rare Diseases|June 13, 2019
Phenotypic variation between siblings with Metachromatic LeukodystrophySaskia Elgün, Jakob Waibel, Christiane Kehrer, et al.
Cerebellum (London, England)|February 17, 2019
Pattern of Cerebellar Atrophy in Friedreich's Ataxia-Using the SUIT TemplateTobias Lindig, Benjamin Bender, Vinod J Kumar, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|November 4, 2025
Brain delivery of a neurotrophic peptide derived from secreted amyloid precursor protein APPsα as a therapeutic strategy for Alzheimer's diseaseLena Rehra, Susanne Erdinger, Lelia Wagner, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 6, 2022
APPsα Rescues Tau-Induced Synaptic PathologyCharlotte S Bold, Danny Baltissen, Susann Ludewig, et al.
Human Mutation|December 24, 2016
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral SclerosisJulie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Orphanet Journal of Rare Diseases|June 13, 2019
Phenotypic variation between siblings with Metachromatic LeukodystrophySaskia Elgün, Jakob Waibel, Christiane Kehrer, et al.
Cerebellum (London, England)|February 17, 2019
Pattern of Cerebellar Atrophy in Friedreich's Ataxia-Using the SUIT TemplateTobias Lindig, Benjamin Bender, Vinod J Kumar, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|November 4, 2025
Brain delivery of a neurotrophic peptide derived from secreted amyloid precursor protein APPsα as a therapeutic strategy for Alzheimer's diseaseLena Rehra, Susanne Erdinger, Lelia Wagner, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 6, 2022
APPsα Rescues Tau-Induced Synaptic PathologyCharlotte S Bold, Danny Baltissen, Susann Ludewig, et al.
Human Mutation|December 24, 2016
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral SclerosisJulie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, et al.
Pageof 2